@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_head
{
this:
np:hasAssertion
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_assertion
;
np:hasProvenance
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_assertion
a
np:Assertion
.
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_provenance
a
np:Provenance
.
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_assertion
{
miriam-gene:8842
a
ncit:C16612
.
lld:C0278510
a
ncit:C7057
.
dgn-gda:DGNe38f99f25cf3e1efd12ea4e324d77cec
sio:SIO_000628
miriam-gene:8842
,
lld:C0278510
;
a
sio:SIO_001121
.
}
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_provenance
{
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_assertion
dcterms:description
"[Here, we investigated expression and prognostic value of the neural stem cell marker CD133, as well as of the pluripotency genes LIN28 and OCT4 in 37 samples of pediatric medulloblastoma, the most common and challenging type of embryonal tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21725800
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP563671.RA9E7S5pgJNj3GreyG7dEWv6ori04GLbOUXZz33e6n-3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}